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17β-Hydroxysteroid Dehydrogenase Type 1 Inhibition: A Potential Treatment Option for Non-Small Cell Lung Cancer.

Emanuele M GarganoAbdelrahman MohamedAhmed S AbdelsamieGiuseppe Felice MangiatordiHanna DrzewieckaPaweł P JagodzińskiArcangela MazziniChris J van KoppenMatthias W LaschkeNicolotti OrazioAngelo CarottiSandrine Marchais-OberwinklerRolf Wolfgang HartmannMartin Frotscher
Published in: ACS medicinal chemistry letters (2021)
In the face of the clinical challenge posed by non-small cell lung cancer (NSCLC), the present need for new therapeutic approaches is genuine. Up to now, no proof existed that 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1) is a viable target for treating this disease. Synthesis of a rationally designed library of 2,5-disubstituted furan derivatives followed by biological screening led to the discovery of 17β-HSD1 inhibitor 1 , capable of fully inhibiting human NSCLC Calu-1 cell proliferation. Its pharmacological profile renders it eligible for further in vivo studies. The very high selectivity of 1 over 17β-HSD2 was investigated, revealing a rational approach for the design of selective inhibitors. 17β-HSD1 and 1 hold promise in fighting NSCLC.
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